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Published in: Journal of Mammary Gland Biology and Neoplasia 1/2024

Open Access 01-12-2024 | Lactation | Perspective

Using Organoids to Tap Mammary Gland Diversity for Novel Insight

Author: Gat Rauner

Published in: Journal of Mammary Gland Biology and Neoplasia | Issue 1/2024

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Abstract

This article offers a comprehensive perspective on the transformative role of organoid technology on mammary gland biology research across a diverse array of mammalian species.
The mammary gland's unique development and regenerative capabilities render this organ an ideal model for studying developmental evolution, stem cell behavior, and regenerative processes. The discussion extends to the use of cross-species mammary organoids to address key biological inquiries in evolution, tissue regeneration, cancer research, and lactation, highlighting the limitations of traditional mouse models and the benefits of incorporating a more diverse range of animal models.
Advances in organoid biology have been critical in overcoming ethical and practical constraints of in-vivo studies, especially in human research. The generation of human and mouse mammary organoids that faithfully recapitulate in-vivo tissues marks a significant stride in this field. Parallel capabilities are now emerging for other mammals, as well.
Utilizing mammary organoids from various species has the potential to make invaluable contributions to our understanding of mammary gland biology, with implications for regenerative medicine, cancer research, and lactation studies, thereby contributing to advancements in human health, agriculture, and nutrition science.
Literature
2.
go back to reference Morris RJ, et al. Capturing and Profiling Adult Hair Follicle Stem Cells. Nat Biotechnol. 2004;22(4):411–7.PubMedCrossRef Morris RJ, et al. Capturing and Profiling Adult Hair Follicle Stem Cells. Nat Biotechnol. 2004;22(4):411–7.PubMedCrossRef
3.
go back to reference Barker N, et al. Identification of Stem Cells in Small Intestine and Colon by Marker Gene Lgr5. Nature. 2007;449(7165):1003–7.PubMedCrossRef Barker N, et al. Identification of Stem Cells in Small Intestine and Colon by Marker Gene Lgr5. Nature. 2007;449(7165):1003–7.PubMedCrossRef
4.
go back to reference Rauner G, et al. Breast Tissue Regeneration is Driven by Cell-Matrix Interactions Coordinating Multi-Lineage Stem Cell Differentiation Through DDR1. Nat Commun. 2021;12(1):7116.PubMedPubMedCentralCrossRef Rauner G, et al. Breast Tissue Regeneration is Driven by Cell-Matrix Interactions Coordinating Multi-Lineage Stem Cell Differentiation Through DDR1. Nat Commun. 2021;12(1):7116.PubMedPubMedCentralCrossRef
5.
go back to reference Englund JI, et al. Laminin Matrix Adhesion Regulates Basal Mammary Epithelial Cell Identity. J Cell Sci. 2022;135(23):jcs260232.PubMedCrossRef Englund JI, et al. Laminin Matrix Adhesion Regulates Basal Mammary Epithelial Cell Identity. J Cell Sci. 2022;135(23):jcs260232.PubMedCrossRef
6.
go back to reference Kass L, et al. Mammary Epithelial Cell: Influence Of Extracellular Matrix Composition and Organization During Development and Tumorigenesis. Int J Biochem Cell Biol. 2007;39(11):1987–94.PubMedPubMedCentralCrossRef Kass L, et al. Mammary Epithelial Cell: Influence Of Extracellular Matrix Composition and Organization During Development and Tumorigenesis. Int J Biochem Cell Biol. 2007;39(11):1987–94.PubMedPubMedCentralCrossRef
8.
go back to reference Naylor MJ, et al. Ablation of Beta1 Integrin in Mammary Epithelium Reveals a Key Role for Integrin in Glandular Morphogenesis and Differentiation. J Cell Biol. 2005;171(4):717–28.PubMedPubMedCentralCrossRef Naylor MJ, et al. Ablation of Beta1 Integrin in Mammary Epithelium Reveals a Key Role for Integrin in Glandular Morphogenesis and Differentiation. J Cell Biol. 2005;171(4):717–28.PubMedPubMedCentralCrossRef
9.
go back to reference Amend SR, et al. Ten Unanswered Questions in Cancer: “If this is true, what does it imply”? Am J Clin Exp Urol. 2018;6(2):26–31.PubMedPubMedCentral Amend SR, et al. Ten Unanswered Questions in Cancer: “If this is true, what does it imply”? Am J Clin Exp Urol. 2018;6(2):26–31.PubMedPubMedCentral
10.
go back to reference Cardiff RD, Wellings SR. The Comparative Pathology of Human and Mouse Mammary Glands. J Mammary Gland Biol Neoplasia. 1999;4(1):105–22.PubMedCrossRef Cardiff RD, Wellings SR. The Comparative Pathology of Human and Mouse Mammary Glands. J Mammary Gland Biol Neoplasia. 1999;4(1):105–22.PubMedCrossRef
11.
go back to reference Rauner, G., et al., Advancements in Human Breast Organoid Culture: Modeling Complex Tissue Structures and Developmental Insights. bioRxiv, 2023: p. 2023.10.02.560364. Rauner, G., et al., Advancements in Human Breast Organoid Culture: Modeling Complex Tissue Structures and Developmental Insights. bioRxiv, 2023: p. 2023.10.02.560364.
12.
go back to reference Yuan L, et al. Reconstruction of Dynamic Mammary Mini Gland in Vitro for Normal Physiology and Oncogenesis. Nat Methods. 2023;20:2021–33.PubMedCrossRef Yuan L, et al. Reconstruction of Dynamic Mammary Mini Gland in Vitro for Normal Physiology and Oncogenesis. Nat Methods. 2023;20:2021–33.PubMedCrossRef
13.
go back to reference Ganz HM, et al. Generation of Ductal Organoids from Normal Mammary Luminal Cells Reveals Invasive Potential. J Pathol. 2021;255(4):451–63.PubMedCrossRef Ganz HM, et al. Generation of Ductal Organoids from Normal Mammary Luminal Cells Reveals Invasive Potential. J Pathol. 2021;255(4):451–63.PubMedCrossRef
14.
go back to reference Linnemann JR, et al. Quantification of Regenerative Potential in Primary Human Mammary Epithelial Cells. Development. 2015;142(18):3239–51.PubMedPubMedCentral Linnemann JR, et al. Quantification of Regenerative Potential in Primary Human Mammary Epithelial Cells. Development. 2015;142(18):3239–51.PubMedPubMedCentral
18.
go back to reference Rosenbluth JM, et al. Organoid Cultures from Normal and Cancer-Prone Human Breast Tissues Preserve Complex Epithelial Lineages. Nat Commun. 2020;11(1):1711.PubMedPubMedCentralCrossRef Rosenbluth JM, et al. Organoid Cultures from Normal and Cancer-Prone Human Breast Tissues Preserve Complex Epithelial Lineages. Nat Commun. 2020;11(1):1711.PubMedPubMedCentralCrossRef
20.
go back to reference Lee J, et al. Human Breast Organoid Models for Lactation Research. Reproduction Breed. 2023;3(3):125–30.CrossRef Lee J, et al. Human Breast Organoid Models for Lactation Research. Reproduction Breed. 2023;3(3):125–30.CrossRef
22.
go back to reference Lewis SM, Callaway MK, dos Santos CO. Clinical Applications of 3D Normal and Breast Cancer Organoids: a Review of Concepts and Methods. Exp Biol Med. 2022;247(24):2176–83.CrossRef Lewis SM, Callaway MK, dos Santos CO. Clinical Applications of 3D Normal and Breast Cancer Organoids: a Review of Concepts and Methods. Exp Biol Med. 2022;247(24):2176–83.CrossRef
24.
go back to reference Richards Z, et al. Prostate Stroma Increases the Viability and Maintains the Branching Phenotype of Human Prostate Organoids. IScience. 2019;12:304–17.PubMedPubMedCentralCrossRef Richards Z, et al. Prostate Stroma Increases the Viability and Maintains the Branching Phenotype of Human Prostate Organoids. IScience. 2019;12:304–17.PubMedPubMedCentralCrossRef
26.
go back to reference Qu Y, et al. Differentiation of Human Induced Pluripotent Stem Cells to Mammary-Like Organoids. Stem cell Rep. 2017;8(2):205–15.CrossRef Qu Y, et al. Differentiation of Human Induced Pluripotent Stem Cells to Mammary-Like Organoids. Stem cell Rep. 2017;8(2):205–15.CrossRef
28.
go back to reference Kim HY, et al. Expanding the Evo-Devo Toolkit: Generation of 3D mammary Tissue from Diverse Mammals. Development. 2024;151:dev202134.PubMedCrossRef Kim HY, et al. Expanding the Evo-Devo Toolkit: Generation of 3D mammary Tissue from Diverse Mammals. Development. 2024;151:dev202134.PubMedCrossRef
29.
go back to reference Bartlett AP, et al. Establishment and Characterization of Equine Mammary Organoids using a Method Translatable to Other Non-Traditional Model Species. Development. 2022;149(7):dev200412.PubMedCrossRef Bartlett AP, et al. Establishment and Characterization of Equine Mammary Organoids using a Method Translatable to Other Non-Traditional Model Species. Development. 2022;149(7):dev200412.PubMedCrossRef
30.
go back to reference Ellis S, et al. Growth and Morphogenesis of Epithelial cell Organoids from Peripheral and Medial Mammary Parenchyma of Prepubertal Heifers. J Dairy Sci. 2000;83(5):952–61.PubMedCrossRef Ellis S, et al. Growth and Morphogenesis of Epithelial cell Organoids from Peripheral and Medial Mammary Parenchyma of Prepubertal Heifers. J Dairy Sci. 2000;83(5):952–61.PubMedCrossRef
31.
go back to reference Arevalo Turrubiarte M, et al. Phenotypic and Functional Characterization of Two Bovine Mammary Epithelial Cell Lines in 2D and 3D Models. Am J Physiol Cell Physiol. 2016;310(5):C348–56.PubMedCrossRef Arevalo Turrubiarte M, et al. Phenotypic and Functional Characterization of Two Bovine Mammary Epithelial Cell Lines in 2D and 3D Models. Am J Physiol Cell Physiol. 2016;310(5):C348–56.PubMedCrossRef
32.
go back to reference Zhan K, et al. Three-Dimensional Culture System can Induce Expression of Casein in Immortalized Bovine Mammary Epithelial Cells. Anim Sci J. 2017;88(5):817–25.PubMedCrossRef Zhan K, et al. Three-Dimensional Culture System can Induce Expression of Casein in Immortalized Bovine Mammary Epithelial Cells. Anim Sci J. 2017;88(5):817–25.PubMedCrossRef
33.
go back to reference Le Jan C, et al. Mammary Transmission of Caprine Arthritis Encephalitis Virus: a 3D Model for in Vitro Study. Reprod Nutr Dev. 2005;45(4):513–23.PubMedCrossRef Le Jan C, et al. Mammary Transmission of Caprine Arthritis Encephalitis Virus: a 3D Model for in Vitro Study. Reprod Nutr Dev. 2005;45(4):513–23.PubMedCrossRef
34.
35.
go back to reference Martignani E, et al. Bovine Mammary Organoids: A Model to Study Epithelial Mammary Cells. Methods Mol Biol. 2018;1817:137–44.PubMedCrossRef Martignani E, et al. Bovine Mammary Organoids: A Model to Study Epithelial Mammary Cells. Methods Mol Biol. 2018;1817:137–44.PubMedCrossRef
37.
go back to reference Griffiths M, McIntosh D, Coles R. The mammary Gland of the Echidna, Tachyglossus Aculeatus’ with Observations on the Incubation of the Egg and on the Newly-Hatched Young. J Zool. 1969;158(3):371–86.CrossRef Griffiths M, McIntosh D, Coles R. The mammary Gland of the Echidna, Tachyglossus Aculeatus’ with Observations on the Incubation of the Egg and on the Newly-Hatched Young. J Zool. 1969;158(3):371–86.CrossRef
38.
go back to reference Oftedal OT. The Mammary Gland and Its Origin During Synapsid Evolution. J Mammary Gland Biol Neoplasia. 2002;7(3):225–52.PubMedCrossRef Oftedal OT. The Mammary Gland and Its Origin During Synapsid Evolution. J Mammary Gland Biol Neoplasia. 2002;7(3):225–52.PubMedCrossRef
39.
go back to reference Hawke T, Bino G, Kingsford RT. A Silent Demise: Historical Insights into Population Changes of the Iconic Platypus (Ornithorhynchus anatinus). Glob Ecol Conserv. 2019;20:e00720. Hawke T, Bino G, Kingsford RT. A Silent Demise: Historical Insights into Population Changes of the Iconic Platypus (Ornithorhynchus anatinus). Glob Ecol Conserv. 2019;20:e00720.
41.
go back to reference Temple-Smith P, Grant T. Uncertain Breeding: a Short History of Reproduction in Monotremes. Reprod Fertil Dev. 2001;13(7–8):487–97.PubMedCrossRef Temple-Smith P, Grant T. Uncertain Breeding: a Short History of Reproduction in Monotremes. Reprod Fertil Dev. 2001;13(7–8):487–97.PubMedCrossRef
43.
go back to reference Neerukonda M, et al. Functional Evaluation of a Monotreme-Specific Antimicrobial Protein, EchAMP, Against Experimentally Induced Mastitis in Transgenic Mice. Transgenic Res. 2019;28(5–6):573–87.PubMedCrossRef Neerukonda M, et al. Functional Evaluation of a Monotreme-Specific Antimicrobial Protein, EchAMP, Against Experimentally Induced Mastitis in Transgenic Mice. Transgenic Res. 2019;28(5–6):573–87.PubMedCrossRef
44.
go back to reference Kumar A, et al. Structural and Mechanistic Insights into EchAMP: A Antimicrobial Protein from the Echidna Milk. Biochim Biophys Acta Biomembr. 2019;1861(6):1260–74.PubMedCrossRef Kumar A, et al. Structural and Mechanistic Insights into EchAMP: A Antimicrobial Protein from the Echidna Milk. Biochim Biophys Acta Biomembr. 2019;1861(6):1260–74.PubMedCrossRef
45.
go back to reference Bisana S, et al. Identification and Functional Characterization of a Novel Monotreme- Specific Antibacterial Protein Expressed During Lactation. PLoS One. 2013;8(1):e53686.PubMedPubMedCentralCrossRef Bisana S, et al. Identification and Functional Characterization of a Novel Monotreme- Specific Antibacterial Protein Expressed During Lactation. PLoS One. 2013;8(1):e53686.PubMedPubMedCentralCrossRef
46.
go back to reference Newman J, et al. Structural Characterization of a Novel Monotreme-Specific Protein with Antimicrobial Activity from the Milk of the Platypus. Acta Crystallogr F Struct Biol Commun. 2018;74(Pt 1):39–45.PubMedPubMedCentralCrossRef Newman J, et al. Structural Characterization of a Novel Monotreme-Specific Protein with Antimicrobial Activity from the Milk of the Platypus. Acta Crystallogr F Struct Biol Commun. 2018;74(Pt 1):39–45.PubMedPubMedCentralCrossRef
47.
go back to reference Enjapoori AK, et al. Monotreme Lactation Protein is Highly Expressed in Monotreme Milk and Provides Antimicrobial Protection. Genome Biol Evol. 2014;6(10):2754–73.PubMedPubMedCentralCrossRef Enjapoori AK, et al. Monotreme Lactation Protein is Highly Expressed in Monotreme Milk and Provides Antimicrobial Protection. Genome Biol Evol. 2014;6(10):2754–73.PubMedPubMedCentralCrossRef
48.
go back to reference Eldridge MDB, et al. An Emerging Consensus in the Evolution, Phylogeny, and Systematics of Marsupials and their Fossil Relatives (Metatheria). J Mammal. 2019;100(3):802–37.CrossRef Eldridge MDB, et al. An Emerging Consensus in the Evolution, Phylogeny, and Systematics of Marsupials and their Fossil Relatives (Metatheria). J Mammal. 2019;100(3):802–37.CrossRef
49.
go back to reference Schep R, et al. Control of Hoxd Gene Transcription in the Mammary Bud by Hijacking a Preexisting Regulatory Landscape. Proc Natl Acad Sci. 2016;113(48):E7720–9.PubMedPubMedCentralCrossRef Schep R, et al. Control of Hoxd Gene Transcription in the Mammary Bud by Hijacking a Preexisting Regulatory Landscape. Proc Natl Acad Sci. 2016;113(48):E7720–9.PubMedPubMedCentralCrossRef
50.
go back to reference Tian R, et al. Molecular Evolution of Vision-Related Genes may Contribute to Marsupial Photic Niche Adaptations. Front Ecol Evol. 2022;10:982073.CrossRef Tian R, et al. Molecular Evolution of Vision-Related Genes may Contribute to Marsupial Photic Niche Adaptations. Front Ecol Evol. 2022;10:982073.CrossRef
51.
go back to reference Long CA. The origin and Evolution of Mammary Glands. Bioscience. 1969;19(6):519–23.CrossRef Long CA. The origin and Evolution of Mammary Glands. Bioscience. 1969;19(6):519–23.CrossRef
52.
53.
go back to reference Lincoln DW, Renfree MB. Mammary Gland Growth and Milk Ejection in the Agile Wallaby, Macropus agilis, Displaying Concurrent Asynchronous Lactation. J Reprod Fertil. 1981;63(1):193–203.PubMedCrossRef Lincoln DW, Renfree MB. Mammary Gland Growth and Milk Ejection in the Agile Wallaby, Macropus agilis, Displaying Concurrent Asynchronous Lactation. J Reprod Fertil. 1981;63(1):193–203.PubMedCrossRef
54.
go back to reference Nicholas KR. Asynchronous Dual Lactation in a Marsupial, the Tammar Wallaby (Macropus eugenii). Biochem Biophys Res Commun. 1988;154(2):529–36.PubMedCrossRef Nicholas KR. Asynchronous Dual Lactation in a Marsupial, the Tammar Wallaby (Macropus eugenii). Biochem Biophys Res Commun. 1988;154(2):529–36.PubMedCrossRef
55.
go back to reference Lemon M, Bailey L. A Specific Protein Difference in the Milk from Two Mammary Glands of a Red Kangaroo. Aust J Exp Biol Med Sci. 1966;44(6):705–8.PubMedCrossRef Lemon M, Bailey L. A Specific Protein Difference in the Milk from Two Mammary Glands of a Red Kangaroo. Aust J Exp Biol Med Sci. 1966;44(6):705–8.PubMedCrossRef
56.
go back to reference Wanyonyi SS, et al. Transcriptome Analysis of Mammary Epithelial Cell Gene Expression Reveals Novel Roles of the Extracellular Matrix. Biochem Biophys Rep. 2017;12:120–8.PubMedPubMedCentral Wanyonyi SS, et al. Transcriptome Analysis of Mammary Epithelial Cell Gene Expression Reveals Novel Roles of the Extracellular Matrix. Biochem Biophys Rep. 2017;12:120–8.PubMedPubMedCentral
57.
go back to reference Wanyonyi SS, et al. The Extracellular Matrix Locally Regulates Asynchronous Concurrent Lactation in Tammar Wallaby (Macropus eugenii). Matrix Biol. 2013;32(6):342–51.PubMedCrossRef Wanyonyi SS, et al. The Extracellular Matrix Locally Regulates Asynchronous Concurrent Lactation in Tammar Wallaby (Macropus eugenii). Matrix Biol. 2013;32(6):342–51.PubMedCrossRef
58.
go back to reference Wanyonyi SS, et al. The Extracellular Matrix Regulates Maeucath1a Gene Expression. Dev Comp Immunol. 2013;40(3–4):289–99.PubMedCrossRef Wanyonyi SS, et al. The Extracellular Matrix Regulates Maeucath1a Gene Expression. Dev Comp Immunol. 2013;40(3–4):289–99.PubMedCrossRef
59.
go back to reference Gupta PB, et al. Phenotypic Plasticity: Driver of Cancer Initiation, Progression, and Therapy Resistance. Cell Stem Cell. 2019;24(1):65–78.PubMedCrossRef Gupta PB, et al. Phenotypic Plasticity: Driver of Cancer Initiation, Progression, and Therapy Resistance. Cell Stem Cell. 2019;24(1):65–78.PubMedCrossRef
61.
go back to reference Nolan E, Lindeman GJ, Visvader JE. Deciphering Breast Cancer: from Biology to the Clinic. Cell. 2023;186(8):1708–28.PubMedCrossRef Nolan E, Lindeman GJ, Visvader JE. Deciphering Breast Cancer: from Biology to the Clinic. Cell. 2023;186(8):1708–28.PubMedCrossRef
63.
go back to reference Luo M, Brooks M, Wicha MS. Epithelial-Mesenchymal Plasticity of Breast Cancer Stem Cells: Implications For Metastasis and Therapeutic Resistance. Curr Pharm Des. 2015;21(10):1301–10.PubMedPubMedCentralCrossRef Luo M, Brooks M, Wicha MS. Epithelial-Mesenchymal Plasticity of Breast Cancer Stem Cells: Implications For Metastasis and Therapeutic Resistance. Curr Pharm Des. 2015;21(10):1301–10.PubMedPubMedCentralCrossRef
64.
go back to reference Bouras T, et al. Notch Signaling Regulates Mammary Stem Cell Function and Luminal Cell-Fate Commitment. Cell Stem Cell. 2008;3(4):429–41.PubMedCrossRef Bouras T, et al. Notch Signaling Regulates Mammary Stem Cell Function and Luminal Cell-Fate Commitment. Cell Stem Cell. 2008;3(4):429–41.PubMedCrossRef
65.
go back to reference Melchor L, et al. Identification of Cellular and Genetic Drivers of Breast Cancer Heterogeneity in Genetically Engineered Mouse Tumour Models. J Pathol. 2014;233(2):124–37.PubMedCrossRef Melchor L, et al. Identification of Cellular and Genetic Drivers of Breast Cancer Heterogeneity in Genetically Engineered Mouse Tumour Models. J Pathol. 2014;233(2):124–37.PubMedCrossRef
66.
go back to reference Bittner JJ. Some Possible Effects of Nursing on the Mammary Gland Tumor Incidence in Mice. Science. 1936;84(2172):162.PubMedCrossRef Bittner JJ. Some Possible Effects of Nursing on the Mammary Gland Tumor Incidence in Mice. Science. 1936;84(2172):162.PubMedCrossRef
68.
go back to reference Callahan R, Smith GH. The Mouse as a Model for Mammary Tumorigenesis: History and Current Aspects. J Mammary Gland Biol Neoplasia. 2008;13(3):269–269.PubMedCrossRef Callahan R, Smith GH. The Mouse as a Model for Mammary Tumorigenesis: History and Current Aspects. J Mammary Gland Biol Neoplasia. 2008;13(3):269–269.PubMedCrossRef
70.
go back to reference Munson L, Moresco A. Comparative Pathology of Mammary Gland Cancers in Domestic and wild Animals. Breast Dis. 2007;28:7–21.PubMedCrossRef Munson L, Moresco A. Comparative Pathology of Mammary Gland Cancers in Domestic and wild Animals. Breast Dis. 2007;28:7–21.PubMedCrossRef
71.
go back to reference Casey HW, Giles RC, Kwapien RP. Mammary Neoplasia in Animals: Pathologic Aspects and the Effects of Contraceptive steroids. Recent Results Cancer Res. 1979;66:129–60.PubMed Casey HW, Giles RC, Kwapien RP. Mammary Neoplasia in Animals: Pathologic Aspects and the Effects of Contraceptive steroids. Recent Results Cancer Res. 1979;66:129–60.PubMed
72.
go back to reference Rauner G, Ledet MM, Van de Walle GR. Conserved and Variable: Understanding Mammary Stem Cells Across Species. Cytometry A. 2018;93(1):125–36.PubMedCrossRef Rauner G, Ledet MM, Van de Walle GR. Conserved and Variable: Understanding Mammary Stem Cells Across Species. Cytometry A. 2018;93(1):125–36.PubMedCrossRef
73.
go back to reference Peaker M. Dairy Animals and Breast Cancer: Reflections on a Long-Term Study From the 1970s that was Never Done. J Dairy Res. 2023;90(1):26–7.CrossRef Peaker M. Dairy Animals and Breast Cancer: Reflections on a Long-Term Study From the 1970s that was Never Done. J Dairy Res. 2023;90(1):26–7.CrossRef
74.
go back to reference Harman RM, et al. miRNA-214-3p Stimulates Carcinogen-Induced Mammary Epithelial Cell Apoptosis in Mammary Cancer-Resistant Species. Commun Biol. 2023;6(1):1006.PubMedPubMedCentralCrossRef Harman RM, et al. miRNA-214-3p Stimulates Carcinogen-Induced Mammary Epithelial Cell Apoptosis in Mammary Cancer-Resistant Species. Commun Biol. 2023;6(1):1006.PubMedPubMedCentralCrossRef
75.
go back to reference Ledet MM, et al. Differential Signaling Pathway Activation in 7,12-Dimethylbenz[a] Anthracene (DMBA)-Treated Mammary Stem/Progenitor Cells from Species with Varying Mammary Cancer Incidence. Oncotarget. 2018;9(67):32761–74.PubMedPubMedCentralCrossRef Ledet MM, et al. Differential Signaling Pathway Activation in 7,12-Dimethylbenz[a] Anthracene (DMBA)-Treated Mammary Stem/Progenitor Cells from Species with Varying Mammary Cancer Incidence. Oncotarget. 2018;9(67):32761–74.PubMedPubMedCentralCrossRef
76.
go back to reference Harman RM, et al. Beyond Tradition and Convention: Benefits of Non-Traditional Model Organisms in Cancer Research. Cancer Metastasis Rev. 2021;40(1):47–69.PubMedCrossRef Harman RM, et al. Beyond Tradition and Convention: Benefits of Non-Traditional Model Organisms in Cancer Research. Cancer Metastasis Rev. 2021;40(1):47–69.PubMedCrossRef
77.
go back to reference Van Keymeulen A, et al. Distinct Stem Cells Contribute to Mammary Gland Development and Maintenance. Nature. 2011;479(7372):189–93.PubMedCrossRef Van Keymeulen A, et al. Distinct Stem Cells Contribute to Mammary Gland Development and Maintenance. Nature. 2011;479(7372):189–93.PubMedCrossRef
78.
go back to reference Davis FM, et al. Single-Cell Lineage Tracing in the Mammary Gland Reveals Stochastic Clonal Dispersion of Stem/Progenitor Cell Progeny. Nat Commun. 2016;7(1):13053.PubMedPubMedCentralCrossRef Davis FM, et al. Single-Cell Lineage Tracing in the Mammary Gland Reveals Stochastic Clonal Dispersion of Stem/Progenitor Cell Progeny. Nat Commun. 2016;7(1):13053.PubMedPubMedCentralCrossRef
80.
81.
go back to reference Van Keymeulen A, et al. Lineage-Restricted Mammary Stem Cells Sustain the Development, Homeostasis, and Regeneration of the Estrogen Receptor Positive Lineage. Cell Rep. 2017;20(7):1525–32.PubMedPubMedCentralCrossRef Van Keymeulen A, et al. Lineage-Restricted Mammary Stem Cells Sustain the Development, Homeostasis, and Regeneration of the Estrogen Receptor Positive Lineage. Cell Rep. 2017;20(7):1525–32.PubMedPubMedCentralCrossRef
82.
83.
go back to reference Rios AC, et al. In situ Identification of Bipotent Stem Cells in the Mammary Gland. Nature. 2014;506(7488):322–7.PubMedCrossRef Rios AC, et al. In situ Identification of Bipotent Stem Cells in the Mammary Gland. Nature. 2014;506(7488):322–7.PubMedCrossRef
84.
go back to reference Cereser B, et al. Analysis of Clonal Expansions Through the Normal and Premalignant Human Breast Epithelium Reveals the Presence of Luminal Stem Cells. J Pathol. 2018;244(1):61–70.PubMedCrossRef Cereser B, et al. Analysis of Clonal Expansions Through the Normal and Premalignant Human Breast Epithelium Reveals the Presence of Luminal Stem Cells. J Pathol. 2018;244(1):61–70.PubMedCrossRef
85.
go back to reference Watson C, Kreuzaler P. Remodeling Mechanisms of the Mammary Gland During Involution. Int J Dev Biol. 2011;55(7-8–9):757–62.PubMedCrossRef Watson C, Kreuzaler P. Remodeling Mechanisms of the Mammary Gland During Involution. Int J Dev Biol. 2011;55(7-8–9):757–62.PubMedCrossRef
86.
go back to reference Chapman RS, et al. Suppression of Epithelial Apoptosis and Delayed Mammary Gland Involution in Mice With a Conditional Knockout Of Stat3. Genes Dev. 1999;13(19):2604–16.PubMedPubMedCentralCrossRef Chapman RS, et al. Suppression of Epithelial Apoptosis and Delayed Mammary Gland Involution in Mice With a Conditional Knockout Of Stat3. Genes Dev. 1999;13(19):2604–16.PubMedPubMedCentralCrossRef
87.
go back to reference Sargeant TJ, et al. Stat3 Controls Cell Death During Mammary Gland Involution by Regulating Uptake of Milk Fat Globules and Lysosomal Membrane Permeabilization. Nat Cell Biol. 2014;16(11):1057–68.PubMedPubMedCentralCrossRef Sargeant TJ, et al. Stat3 Controls Cell Death During Mammary Gland Involution by Regulating Uptake of Milk Fat Globules and Lysosomal Membrane Permeabilization. Nat Cell Biol. 2014;16(11):1057–68.PubMedPubMedCentralCrossRef
89.
go back to reference Li M, et al. Mammary-Derived Signals Activate Programmed Cell Death During the First Stage of Mammary Gland Involution. Proc Natl Acad Sci U S A. 1997;94(7):3425–30.PubMedPubMedCentralCrossRef Li M, et al. Mammary-Derived Signals Activate Programmed Cell Death During the First Stage of Mammary Gland Involution. Proc Natl Acad Sci U S A. 1997;94(7):3425–30.PubMedPubMedCentralCrossRef
90.
go back to reference Sharp JA, et al. Fur Seal Adaptations to Lactation: Insights into Mammary Gland Function. Curr Top Dev Biol. 2006;72:275–308.PubMedCrossRef Sharp JA, et al. Fur Seal Adaptations to Lactation: Insights into Mammary Gland Function. Curr Top Dev Biol. 2006;72:275–308.PubMedCrossRef
91.
go back to reference Sharp JA, Lefèvre C, Nicholas KR. Lack of Functional Alpha-Lactalbumin Prevents Involution in Cape Fur Seals and Identifies the Protein As an Apoptotic Milk Factor in Mammary Gland Involution. BMC Biol. 2008;6:48.PubMedPubMedCentralCrossRef Sharp JA, Lefèvre C, Nicholas KR. Lack of Functional Alpha-Lactalbumin Prevents Involution in Cape Fur Seals and Identifies the Protein As an Apoptotic Milk Factor in Mammary Gland Involution. BMC Biol. 2008;6:48.PubMedPubMedCentralCrossRef
92.
go back to reference Sharp JA, et al. Dimeric but not Monomeric α-Lactalbumin Potentiates Apoptosis by up Regulation of ATF3 and Reduction of Histone Deacetylase Activity in Primary and Immortalised Cells. Cell Signal. 2017;33:86–97.PubMedCrossRef Sharp JA, et al. Dimeric but not Monomeric α-Lactalbumin Potentiates Apoptosis by up Regulation of ATF3 and Reduction of Histone Deacetylase Activity in Primary and Immortalised Cells. Cell Signal. 2017;33:86–97.PubMedCrossRef
93.
go back to reference Durham SD, et al. Creation of a Milk Oligosaccharide Database, MilkOligoDB, Reveals Common Structural Motifs and Extensive Diversity Across Mammals. Sci Rep. 2023;13(1):10345.PubMedPubMedCentralCrossRef Durham SD, et al. Creation of a Milk Oligosaccharide Database, MilkOligoDB, Reveals Common Structural Motifs and Extensive Diversity Across Mammals. Sci Rep. 2023;13(1):10345.PubMedPubMedCentralCrossRef
97.
go back to reference Lefèvre CM, Sharp JA, Nicholas KR. Evolution of Lactation: Ancient Origin and Extreme Adaptations of the Lactation System. Annu Rev Genomics Hum Genet. 2010;11:219–38.PubMedCrossRef Lefèvre CM, Sharp JA, Nicholas KR. Evolution of Lactation: Ancient Origin and Extreme Adaptations of the Lactation System. Annu Rev Genomics Hum Genet. 2010;11:219–38.PubMedCrossRef
98.
go back to reference Sharp JA, et al. The tammar wallaby: A Marsupial Model to Examine the Timed Delivery and Role of Bioactives in Milk. Gen Comp Endocrinol. 2017;244:164–77.PubMedPubMedCentralCrossRef Sharp JA, et al. The tammar wallaby: A Marsupial Model to Examine the Timed Delivery and Role of Bioactives in Milk. Gen Comp Endocrinol. 2017;244:164–77.PubMedPubMedCentralCrossRef
99.
101.
go back to reference Urashima T, et al. Recent Advances in Studies on Milk Oligosaccharides of Cows and Other Domestic Farm Animals. Biosci Biotechnol Biochem. 2013;77:455–66.PubMedCrossRef Urashima T, et al. Recent Advances in Studies on Milk Oligosaccharides of Cows and Other Domestic Farm Animals. Biosci Biotechnol Biochem. 2013;77:455–66.PubMedCrossRef
102.
go back to reference Asakuma S., et al., Variation of Major Neutral Oligosaccharides Levels in Human Colostrum. Eur J Clin Nutr. 2007. Asakuma S., et al., Variation of Major Neutral Oligosaccharides Levels in Human Colostrum. Eur J Clin Nutr. 2007.
103.
go back to reference Kunz C, et al. Lactose-Derived Oligosaccharides in the Milk of Elephants: Comparison With Human Milk. Br J Nutr. 1999;82:391–9.PubMedCrossRef Kunz C, et al. Lactose-Derived Oligosaccharides in the Milk of Elephants: Comparison With Human Milk. Br J Nutr. 1999;82:391–9.PubMedCrossRef
104.
go back to reference Green B, Merchant J, Newgrain K. Milk Composition in the Eastern Quoll, Dasyurus Viverrinus (Marsupialia:Dasyuridae). Aust J Biol Sci. 1987;40(4):379–87.PubMedCrossRef Green B, Merchant J, Newgrain K. Milk Composition in the Eastern Quoll, Dasyurus Viverrinus (Marsupialia:Dasyuridae). Aust J Biol Sci. 1987;40(4):379–87.PubMedCrossRef
105.
go back to reference Messer M, et al. Changes in Milk Carbohydrates During Lactation in the Eastern Quoll, Dasyurus Viverrinus (Marsupialia). Comp Biochem Physiol B. 1987;88(4):1083–6.PubMedCrossRef Messer M, et al. Changes in Milk Carbohydrates During Lactation in the Eastern Quoll, Dasyurus Viverrinus (Marsupialia). Comp Biochem Physiol B. 1987;88(4):1083–6.PubMedCrossRef
107.
go back to reference German JB, et al. Human Milk Oligosaccharides: Evolution, Structures and Bioselectivity as Substrates for Intestinal Bacteria. Nestle Nutr Workshop Ser Pediatr Program. 2008;62:205–18 discussion 218-22.PubMedPubMedCentralCrossRef German JB, et al. Human Milk Oligosaccharides: Evolution, Structures and Bioselectivity as Substrates for Intestinal Bacteria. Nestle Nutr Workshop Ser Pediatr Program. 2008;62:205–18 discussion 218-22.PubMedPubMedCentralCrossRef
108.
go back to reference Tsugami Y, et al. Establishment of an in Vitro Culture Model to Study Milk Production and the Blood-Milk Barrier with Bovine Mammary Epithelial Cells. Anim Sci J. 2020;91(1):e13355.PubMedCrossRef Tsugami Y, et al. Establishment of an in Vitro Culture Model to Study Milk Production and the Blood-Milk Barrier with Bovine Mammary Epithelial Cells. Anim Sci J. 2020;91(1):e13355.PubMedCrossRef
109.
go back to reference Wu RY, et al. Variations in the Composition of Human Milk Oligosaccharides Correlates with Effects on Both the Intestinal Epithelial Barrier and Host Inflammation: A Pilot Study. Nutrients. 2022;14(5):1014.PubMedPubMedCentralCrossRef Wu RY, et al. Variations in the Composition of Human Milk Oligosaccharides Correlates with Effects on Both the Intestinal Epithelial Barrier and Host Inflammation: A Pilot Study. Nutrients. 2022;14(5):1014.PubMedPubMedCentralCrossRef
Metadata
Title
Using Organoids to Tap Mammary Gland Diversity for Novel Insight
Author
Gat Rauner
Publication date
01-12-2024
Publisher
Springer US
Keyword
Lactation
Published in
Journal of Mammary Gland Biology and Neoplasia / Issue 1/2024
Print ISSN: 1083-3021
Electronic ISSN: 1573-7039
DOI
https://doi.org/10.1007/s10911-024-09559-z

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